Pharmaceutical SAS Programmer - (US-PA-Swiftwater - 18370)

Minimum Education: Tech School
Job Type: Full Time
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This is a rare opportunity for someone who is looking to work for one of most successful bio-pharmaceutical companies. Be the first programmer to join this newly established group and assist with their expansion.
As the Lead/ Sr SAS programmer, you will:
1. Provide general SAS programming support to Clinical Research and Development
2. Under the direction of a statistician, generate tables, listings and graphs for interim analyses, preliminary reports and Final Clinical/Statistical Reports for in-house use, publications, or regulatory submissions.
3. Provide input regarding improvements and enhancements to an existing SAS macro library.
4. Work as part of the clinical team in the preparation of table/listing/figure shells in the statistical analysis plan.
5. Validate the work of other programmers.
6. Prepare SAS datasets and appropriate documentation for electronic submissions.

2 plus years Pharmaceutical or CRO industry experience as a SAS programmer supporting clinical trials for regulatory submissions
In depth knowledge of all relevant SAS procedures and processes including interfaces with other systems (EXCEL, MS Word tables, Oracle Clinical).
Clinical trial design, clinical trial statistics.
Fundamentals of Oracle Clinical and SQL a strong plus
Excellent interpersonal, written and oral communication, and organizational skills. Team player
Pharmaceutical SAS Programmer
Pharmaceutical SAS Programmer
Pharmaceutical SAS Programmer